FDA UDI Not in Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780248231 · Model: 1222MAINKIT · Ascension Orthopedics, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780248231
Version / Model
1222MAINKIT
Catalog Number
1222MAINKIT
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-05
Public Version
3
Public Version Date
2023-05-02
Public Version Status
Update
Public Device Record Key
8626591f-a777-4ca8-82a6-361122ded8db
Distribution End Date
2023-03-31

Device Description

Integra® External Fixation System The Maintenance Kit consists of a 10mm and 13mm box wrench, a universal bolt tubular wrench, a pivoting socket wrench, and a k-wire guide. These instruments are used with the Integra External Fixation System.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HXC WRENCH
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
35647 External orthopaedic fixation system, reusable

Identifiers

Type ID
Secondary M2691222MAINTKIT1
Primary 10381780248231

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify N/A